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Completed Phase 1Phase 2 Interventional Accepts healthy volunteers Results available

A Study on the Immune Response and Safety of an Adjuvanted Human Papillomavirus Vaccine When Given to Healthy Women 16 to 26 Years of Age

ClinicalTrials.gov ID: NCT05496231

Public ClinicalTrials.gov record NCT05496231. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 5:41 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1/2 Randomized, Observer-blinded, Multi-country Study to Evaluate Safety and Immunogenicity of Investigational Adjuvanted Human Papillomavirus Vaccine in Females (16 to 26 Years of Age)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The main purpose of this study was to evaluate the safety and reactogenicity of GlaxoSmithKline Biologicals SA (GSK)'s investigational adjuvanted human papillomavirus (HPV) vaccine formulations.

Study identification

NCT ID
NCT05496231
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
1,080 participants

Conditions and interventions

Eligibility (public fields only)

Age range
16 Years to 26 Years
Sex
Female
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 22, 2022 (Actual)
Primary completion
Feb 23, 2024 (Actual)
Completion
Feb 25, 2024 (Actual)
Last update posted
Feb 3, 2025

2022 – 2024

United States locations

U.S. sites
39
U.S. states
21
U.S. cities
36
Facility City State ZIP Site status
GSK Investigational Site San Diego California 92103-6204 —
GSK Investigational Site San Diego California 92120 —
GSK Investigational Site Wheat Ridge Colorado 80033 —
GSK Investigational Site Coral Gables Florida 33134 —
GSK Investigational Site Kissimmee Florida 34741 —
GSK Investigational Site Miami Florida 33125 —
GSK Investigational Site North Miami Beach Florida 33162 —
GSK Investigational Site Pompano Beach Florida 33060 —
GSK Investigational Site Sarasota Florida 34239 —
GSK Investigational Site Atlanta Georgia 30328 —
GSK Investigational Site Evansville Indiana 47712 —
GSK Investigational Site South Bend Indiana 46617 —
GSK Investigational Site Topeka Kansas 66606 —
GSK Investigational Site Wichita Kansas 67205 —
GSK Investigational Site Lexington Kentucky 40509 —
GSK Investigational Site Covington Louisiana 70433 —
GSK Investigational Site Elkridge Maryland 21075 —
GSK Investigational Site Saginaw Michigan 48602 —
GSK Investigational Site Jefferson City Missouri 65109 —
GSK Investigational Site Las Vegas Nevada 89102 —
GSK Investigational Site Albuquerque New Mexico 87102 —
GSK Investigational Site Raleigh North Carolina 27612 —
GSK Investigational Site Columbus Ohio 43213 —
GSK Investigational Site Norman Oklahoma 73072 —
GSK Investigational Site North Charleston South Carolina 29405 —
GSK Investigational Site Chattanooga Tennessee 37404 —
GSK Investigational Site Carrollton Texas 75010 —
GSK Investigational Site Corpus Christi Texas 78412 —
GSK Investigational Site Dallas Texas 75251 —
GSK Investigational Site Fort Worth Texas 76104 —
GSK Investigational Site Houston Texas 77065 —
GSK Investigational Site Humble Texas 77338 —
GSK Investigational Site Humble Texas 77346 —
GSK Investigational Site Irving Texas 75062 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site Tomball Texas 77375 —
GSK Investigational Site West Jordan Utah 84088 —
GSK Investigational Site Norfolk Virginia 23502 —
GSK Investigational Site Norfolk Virginia 68701 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 29 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05496231, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 3, 2025 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05496231 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →